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  5. NDC Package Code: 51285-367-01 Trexall

NDC Package 51285-367-01 Trexall

Methotrexate Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51285-367-01
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
51285-367
Proprietary Name:
Trexall
Non-Proprietary Name:
Methotrexate
Substance Name:
Methotrexate Sodium
Usage Information:
Methotrexate is used to treat certain types of cancer or to control severe psoriasis or rheumatoid arthritis that has not responded to other treatments. It may also be used to control juvenile rheumatoid arthritis. Methotrexate belongs to a class of drugs known as antimetabolites. It works by slowing or stopping the growth of cancer cells and suppressing the immune system. Early treatment of rheumatoid arthritis with more aggressive therapy such as methotrexate helps to reduce further joint damage and to preserve joint function.
11-Digit NDC Billing Format:
51285036701
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 105586 - methotrexate 10 MG Oral Tablet
  • RxCUI: 283510 - methotrexate 15 MG Oral Tablet
  • RxCUI: 283511 - methotrexate 5 MG Oral Tablet
  • RxCUI: 283671 - methotrexate 7.5 MG Oral Tablet
  • RxCUI: 284592 - Trexall 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Teva Women's Health, Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • METHOTREXATE SODIUM 7.5 mg/1
    • Pharmacologic Class(es):
  • Folate Analog Metabolic Inhibitor - [EPC] (Established Pharmacologic Class)
  • Folic Acid Metabolism Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA040385
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-03-2001
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 51285-367-01 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    51285036701J8610Methotrexate oral 2.5 mg2.5 MG3019090

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51285-367-01?

    The NDC Packaged Code 51285-367-01 is assigned to a package of 30 tablet, film coated in 1 bottle of Trexall, a human prescription drug labeled by Teva Women's Health, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

    Is NDC 51285-367 included in the NDC Directory?

    Yes, Trexall with product code 51285-367 is active and included in the NDC Directory. The product was first marketed by Teva Women's Health, Inc. on May 03, 2001 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 51285-367-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

    What is the 11-digit format for NDC 51285-367-01?

    The 11-digit format is 51285036701. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-251285-367-015-4-251285-0367-01